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Gender disparity in cases enrolled in clinical trials of visceral leishmaniasis: A systematic review and meta-analysis
BACKGROUND: A higher caseload of visceral leishmaniasis (VL) has been observed among males in community-based surveys. We carried out this review to investigate how the observed disparity in gender distribution is reflected in clinical trials of antileishmanial therapies. METHODS: We identified rele...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7963105/ https://www.ncbi.nlm.nih.gov/pubmed/33725005 http://dx.doi.org/10.1371/journal.pntd.0009204 |
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author | Dahal, Prabin Singh-Phulgenda, Sauman Olliaro, Piero L. Guerin, Philippe J. |
author_facet | Dahal, Prabin Singh-Phulgenda, Sauman Olliaro, Piero L. Guerin, Philippe J. |
author_sort | Dahal, Prabin |
collection | PubMed |
description | BACKGROUND: A higher caseload of visceral leishmaniasis (VL) has been observed among males in community-based surveys. We carried out this review to investigate how the observed disparity in gender distribution is reflected in clinical trials of antileishmanial therapies. METHODS: We identified relevant studies by searching a database of all published clinical trials in VL from 1980 through 2019 indexed in the Infectious Diseases Data Observatory (IDDO) VL clinical trials library. The proportion of male participants enrolled in studies eligible for inclusion in this review were extracted and combined using random effects meta-analysis of proportion. Results were expressed as percentages and presented with respective 95% confidence intervals (95% CIs). Heterogeneity was quantified using I(2) statistics and sub-group meta-analyses were carried out to explore the sources of heterogeneity. RESULTS: We identified 135 published studies (1980–2019; 32,177 patients) with 68.0% [95% CI: 65.9%–70.0%; I(2) = 92.6%] of the enrolled participants being males. The corresponding estimates were 67.6% [95% CI: 65.5%–69.7%; n = 91 trials; I(2) = 90.5%; 24,218 patients] in studies conducted in the Indian sub-continent and 74.1% [95% CI: 68.4%–79.1%; n = 24 trials; I(2) = 94.4%; 6,716 patients] in studies from Eastern Africa. The proportion of male participants was 57.9% [95% CI: 54.2%–61.5%] in studies enrolling children aged <15 years, 78.2% [95% CI: 66.0%–86.9%] in studies that enrolled adults (≥15 years), and 68.1% [95% CI: 65.9%–70.0%] in studies that enrolled patients of all ages. There was a trend for decreased proportions of males enrolled over time: 77.1% [95% CI: 70.2%–82.8%; 1356 patients] in studies published prior to the 1990s whereas 64.3% [95% CI: 60.3%–68.2%; 15,611 patients] in studies published on or after 2010. In studies that allowed the inclusion of patients with HIV co-infections, 76.5% [95% CI: 63.8%–85.9%; 5,123 patients] were males and the corresponding estimate was 64.0% [95% CI: 61.4%–66.5% 17,500 patients] in studies which excluded patients with HIV co-infections. CONCLUSIONS: Two-thirds of the participants enrolled in clinical studies in VL conducted in the past 40 years were males, though the imbalance was less in children and in more recent trials. VL treatment guidelines are informed by the knowledge of treatment outcomes from a population that is heavily skewed towards adult males. Investigators planning future studies should consider this fact and ensure approaches for more gender-balanced inclusion. |
format | Online Article Text |
id | pubmed-7963105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-79631052021-03-26 Gender disparity in cases enrolled in clinical trials of visceral leishmaniasis: A systematic review and meta-analysis Dahal, Prabin Singh-Phulgenda, Sauman Olliaro, Piero L. Guerin, Philippe J. PLoS Negl Trop Dis Research Article BACKGROUND: A higher caseload of visceral leishmaniasis (VL) has been observed among males in community-based surveys. We carried out this review to investigate how the observed disparity in gender distribution is reflected in clinical trials of antileishmanial therapies. METHODS: We identified relevant studies by searching a database of all published clinical trials in VL from 1980 through 2019 indexed in the Infectious Diseases Data Observatory (IDDO) VL clinical trials library. The proportion of male participants enrolled in studies eligible for inclusion in this review were extracted and combined using random effects meta-analysis of proportion. Results were expressed as percentages and presented with respective 95% confidence intervals (95% CIs). Heterogeneity was quantified using I(2) statistics and sub-group meta-analyses were carried out to explore the sources of heterogeneity. RESULTS: We identified 135 published studies (1980–2019; 32,177 patients) with 68.0% [95% CI: 65.9%–70.0%; I(2) = 92.6%] of the enrolled participants being males. The corresponding estimates were 67.6% [95% CI: 65.5%–69.7%; n = 91 trials; I(2) = 90.5%; 24,218 patients] in studies conducted in the Indian sub-continent and 74.1% [95% CI: 68.4%–79.1%; n = 24 trials; I(2) = 94.4%; 6,716 patients] in studies from Eastern Africa. The proportion of male participants was 57.9% [95% CI: 54.2%–61.5%] in studies enrolling children aged <15 years, 78.2% [95% CI: 66.0%–86.9%] in studies that enrolled adults (≥15 years), and 68.1% [95% CI: 65.9%–70.0%] in studies that enrolled patients of all ages. There was a trend for decreased proportions of males enrolled over time: 77.1% [95% CI: 70.2%–82.8%; 1356 patients] in studies published prior to the 1990s whereas 64.3% [95% CI: 60.3%–68.2%; 15,611 patients] in studies published on or after 2010. In studies that allowed the inclusion of patients with HIV co-infections, 76.5% [95% CI: 63.8%–85.9%; 5,123 patients] were males and the corresponding estimate was 64.0% [95% CI: 61.4%–66.5% 17,500 patients] in studies which excluded patients with HIV co-infections. CONCLUSIONS: Two-thirds of the participants enrolled in clinical studies in VL conducted in the past 40 years were males, though the imbalance was less in children and in more recent trials. VL treatment guidelines are informed by the knowledge of treatment outcomes from a population that is heavily skewed towards adult males. Investigators planning future studies should consider this fact and ensure approaches for more gender-balanced inclusion. Public Library of Science 2021-03-16 /pmc/articles/PMC7963105/ /pubmed/33725005 http://dx.doi.org/10.1371/journal.pntd.0009204 Text en © 2021 Dahal et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Dahal, Prabin Singh-Phulgenda, Sauman Olliaro, Piero L. Guerin, Philippe J. Gender disparity in cases enrolled in clinical trials of visceral leishmaniasis: A systematic review and meta-analysis |
title | Gender disparity in cases enrolled in clinical trials of visceral leishmaniasis: A systematic review and meta-analysis |
title_full | Gender disparity in cases enrolled in clinical trials of visceral leishmaniasis: A systematic review and meta-analysis |
title_fullStr | Gender disparity in cases enrolled in clinical trials of visceral leishmaniasis: A systematic review and meta-analysis |
title_full_unstemmed | Gender disparity in cases enrolled in clinical trials of visceral leishmaniasis: A systematic review and meta-analysis |
title_short | Gender disparity in cases enrolled in clinical trials of visceral leishmaniasis: A systematic review and meta-analysis |
title_sort | gender disparity in cases enrolled in clinical trials of visceral leishmaniasis: a systematic review and meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7963105/ https://www.ncbi.nlm.nih.gov/pubmed/33725005 http://dx.doi.org/10.1371/journal.pntd.0009204 |
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